http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022017891-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73e0d5808f34f512649e277bd216a344
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-1034
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6806
filingDate 2019-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4f4656e380e58fdf67eee2267a8ea4e6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_716442569dadb7e825327a78e7994cca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a48bf16ab4f3fcfe92ebecf66be0817a
publicationDate 2022-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2022017891-A1
titleOfInvention Improvements in variant detection
abstract The present invention provides a method for detecting variant cell-free DNA (cfDNA) in a sample obtained from a subject, where analysis of the sample includes a size-selection step which separates out different fragment sizes of DNA. The sample may be a limited volume sample such as a blood, serum or plasma sample of less than 500 μl (e.g. a blood or plasma sample of about 50 μl), or other sample that has a low content of cfDNA. The sample may have been stored and/or dried and not have been processed to remove cells or cellular material prior to storage. The size-selection step may comprise filtering-out, depleting or removing genomic DNA (gDNA) fragments of >200 bp, >300 bp, >500 bp, >700 bp, >1000 bp, >1200 bp, >1500 bp, or >2000 bp prior to analysis, e.g. prior to DNA sequencing. The method may further comprise performing an analysis that summarises or combines data across multiple loci.
priorityDate 2018-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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